HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722673Generated: October 30, 2026
4-Methylmorpholine → HCID 57035141, compound
https://huagongshe.com/reaction/1722673
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | (isopropylthio)acetic acid | HCID 537958 | — |
| Reactant | HCID 15016692 | HCID 15016692 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57035141 | HCID 57035141 | 50.8% |
Reaction Steps
To (2-propylmercapto)acetic acid (44.3 mg, 0.33 mmol) in the THF (3 mL) at 0°(b) was added N-methylmorpholine (37 microliters, 0.34 mmol) followed by isobutylchloroformate (43 microliters, 0.33 mmol). The mixture was stirred at 0° C. for 15 minutes and (3S,4S)-1-amino-3-hydroxy-4-t-butyloxycarbonylamino-5-cyclohexylpentane (51.0 mg, 0.17 mmol) was added followed by stirring at 0° C. for 15 minutes and at 25° C. for 2 hours. The mixture was poured into ethyl acetate, washed with 0.5 M H3PO4, 2 M Na2SO4 and evaporated to afford 36 mg (50%) of the desired compound. Mass spectrum: (M+1)+ =417.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04857507 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-13a984ef6b20457abac97b0ce9572ef8 |
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| Source note | uspto-grants-1989_08 |
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